Your expertise. A team of specialist agents.
Hover any deliverable pill on the right to trace which sources and agents produce it, or click a pill to jump straight to that workflow.
Aligned with the requirements of EMA, FDA, G-BA, IQWiG, EU HTA / JCA, NICE, HAS — and your own SOPs.
1. You ask
One request in chat, no new tool to learn.
2. Regulaido delegates
The right agents are chosen for you automatically.
3. You review
Every result cited, every step open for sign-off.
The 8 specialists behind it
Each agent has its own domain tools and guardrails.
Regulaido picks the right ones for your request automatically.
Systematic literature research
Systematic literature reviews in Regulaido run in a dedicated six-stage PRISMA 2020 workbench, from Boolean query building and deduplication to dual-stage screening, page-exact PDF extraction, and Risk-of-Bias synthesis, with human sign-off at every gate.
1. Search: Query Builder & Recall Check
Builds Boolean & MeSH search strings across literature databases and verifies that landmark reference trials are captured before screening begins.
2. Deduplicate: Multi-Database Deduplication
Merges duplicate records across PubMed, Embase, Cochrane, and registry imports with full snapshot history and one-click undo.
3. Abstracts: AI-Assisted Abstract Screening
Screens titles and abstracts with verbatim quote highlights, PICO criterion scoring, dual-reviewer conflict resolution, and strict exclusion gates.
4. Full-Text PDFs: Automated PDF Retrieval & Review
Fetches open-access full texts automatically, matches batch-uploaded PDFs to study records, and opens a split-screen full-text eligibility viewer.
5. Extraction: Cited Table Extraction
Populates baseline and endpoint extraction grids where every cell jumps directly to the highlighted paragraph or table row in the source PDF.
6. Synthesis & Export: Risk of Bias & PRISMA Export
Generates Cochrane RoB 2 assessments, living PRISMA 2020 flow diagrams, and exports ready-to-submit Excel extraction workbooks and Word tables.
Word, Excel, Slides & XML
Medical writers work in real office files, not markdown snippets. Regulaido reads, edits, and generates native Word (.docx), Excel (.xlsx), PowerPoint (.pptx), and EMA FHIR ePI (.xml) files directly
inside your workspace.
.DOCXMicrosoft Word
Drafts and edits directly inside your sponsor or consultancy Word templates while preserving styles, headings, cross-references, and embedded figures.
.XLSXMicrosoft Excel
Builds, queries, and edits multi-sheet Excel workbooks with live formulas, baseline/endpoint extraction matrices, and summary charts.
.PPTXMicrosoft PowerPoint
Turns CSRs, protocols, and HTA briefings into executive slide decks in your corporate master theme with native editable charts and tables.
.XML / .PDFEMA FHIR ePI & Cited PDFs
Converts approved Word SmPCs into validated EMA FHIR ePI XML bundles in minutes and links every claim to its exact source PDF passage.
Meet Promptly & Studio tools
Your built-in co-pilot for prompts, templates, and source verification.
Medical writers shouldn’t have to become prompt engineers. Promptly sits right inside your Regulaido workspace to turn rough requests into structured regulatory instructions and guide your team through complex workflows.
“Pimp my Prompt”
Write a quick note or dictate by voice and Promptly expands it with the right regulatory structure, section references, and table formatting rules.
Shared Prompt Library
Save and share validated prompt templates for AMNOG Modul 4, CTD 2.5, CSR synopses, and QC checks across your entire writing department.
Split-Screen PDF Viewer
Click any superscript citation in a chat answer or extracted table cell to open the source PDF at the exact highlighted paragraph and table row.
Pricing
Sized to your team
Flexible licensing from a single writing team to an entire department.
All 8 agents & SLR workbench included
Every specialist agent, systematic literature research, native Office file editors, and Promptly included.
Hands-on onboarding
Workshops and workflow setup on your own templates and document types.
Dedicated EU tenant
ISO/IEC 27001:2022 certified EU hosting with Microsoft Entra ID SSO.
See Regulaido on your own documents.
Bring an SLR protocol, a house Word template, or a dossier section. In 30 minutes we will run it live and answer your questions on workflows, EU hosting, and rollout.
“Tell me which dossier, literature review, or Word template is eating your team’s week. We’ll test it live together.”
